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Rabbit anti-Human HGD Monoclonal Antibody

The antibody against HGD was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 346-445 of human HGD (Q93099) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-13225A

The antibody against HGD was raised in Rabbit using a synthetic peptide corresponding to a sequence within amino acids 346-445 of human HGD (Q93099) as the immunogen. The monoclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-13225A ClonalityMonoclonal
Host SpeciesRabbitTarget NameHGD
Target SynonymsAKU; HGO; HGDFormLiquid
Species ReactivityHumanIsotypeIgG
Storage Buffer50% Glycerol, 0.05% BSA, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesHepG2, HT-29ApplicationELISA, WB

Immunogen Information


Immunogen DescriptionA synthetic peptide corresponding to a sequence within amino acids 346-445 of human HGD (Q93099).Target SpeciesHuman
Immunogen SequenceIRGHYEAKQGGFLPGGGSLHSTMTPHGPDADCFEKASKVKLAPERIADGTMAFMFESSLSLAVTKWGLKASRCLDENYHKCWEPLKSHFTPNSRNPAEPNUniprot IDQ93099
Background Information
  • Uniprot Id

    Q93099

  • Target Species

    Human

  • Target Name

    HGD

  • Target Full Name

    Homogentisate 1,2-dioxygenase

  • Target Involvement

    Alkaptonuria (AKU)

  • Target Protein Families

    Homogentisate dioxygenase family

  • Target Tissue Specificity

    Highest expression in the prostate, small intestine, colon, kidney and liver.

  • Target Synonyms

    2-dioxygenase; AKU; FLJ94126; hgd; HGD_HUMAN; HGO; Homogentisate 1 2 dioxygenase; Homogentisate 1; Homogentisate oxidase; Homogentisate oxygenase; Homogentisic acid oxidase; Homogentisicase

  • Target Background

    This gene encodes the enzyme homogentisate 1, 2 dioxygenase. This enzyme is involved in the catabolism of the amino acids tyrosine and phenylalanine. Mutations in this gene are the cause of the autosomal recessive metabolism disorder alkaptonuria.

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